Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Cellular component
- GO: Biological process
- GO: Molecular function
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: snx29 ENSLOCG00000007467

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Description

sorting nexin 29 [Source:NCBI gene;Acc:102685208]

Location

Chromosome LG13: 14,160,090-14,265,048 forward strand.

LepOcu1:CM001416.1

About this gene

This gene has 1 transcript (splice variant), 208 orthologues and 14 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSLOCT00000009078.1	snx29-201	2421	806aa	ENSLOCP00000009067.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	W5ML08	A single transcript chosen for a gene which is the most conserved, most highly expressed, has the longest coding sequence and is represented in other key resources, such as NCBI and UniProt. This is defined in detail on http://www.ensembl.org/info/genome/genebuild/canonical.htmlEnsembl Canonical,

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Summary

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